The ISTH bleeding assessment tool as predictor of bleeding events in inherited platelet disorders: Communication from the ISTH SSC Subcommittee on Platelet Physiology
2021
Gresele, Paolo | Falcinelli, Emanuela | Bury, Loredana | Pecci, Alessandro | Alessi, Marie‐Christine | Borhany, Munira | Heller, Paula | Santoro, Cristina | Cid, Ana Rosa | Orsini, Sara | Fontana, Pierre | De Candia, Erica | Podda, Gianmarco | Kannan, Meganathan | Jurk, Kerstin | Castaman, Giancarlo | Falaise, Céline | Guglielmini, Giuseppe | Noris, Patrizia | Zaninetti, Carlo | Fiore, Mathieu | Tosetto, Alberto | Zuniga, Pamela | Miyazaki, Koji | Dupuis, Arnaud | Hayward, Catherine | Casonato, Alessandra | Grandone, Elvira | Mazzucconi, Maria Gabriella | James, Paula | Fabris, Fabrizio | Henskens, Yvonne | Napolitano, Mariasanta | Curnow, Jennifer | Gkalea, Vasiliki | Fedor, Marian | Lambert, Michele | Zieger, Barbara | Barcella, Luca | Cosmi, Benilde | Giordano, Paola | Porri, Claudia | Melazzini, Federica | Abid, Madiha | Glembotsky, Ana | Ferrara, Grazia | Russo, Alexandra | Deckmyn, Hans | Frelinger, Andrew | Harrison, Paul | Mezzano, Diego | Mumford, Andrew | Lordkipanidzé, Marie
Background The ISTH Bleeding Assessment Tool (ISTH-BAT) has been validated for clinical screening of suspected von Willebrand disease (VWD) and for bleeding prediction. Recently it has been validated for subjects with inherited platelet disorders (IPD) (BAT-VAL study).Objectives To determine whether the ISTH-BAT bleeding score (BS) predicts subsequent bleeding events requiring treatment in IPD patients.Methods Patients with IPD, type 1 VWD (VWD-1) and age- and sex-matched healthy controls enrolled in the BAT-VAL study were prospectively followed-up for 2 years and bleeding episodes requiring treatment were recorded.Results Of the 1098 subjects initially enrolled, 955 were followed-up and 124 suffered hemorrhages during follow-up, 60% of whom had inherited platelet function disorders (IPFD). Total number of events was significantly higher in IPFD (n = 235) than VWD-1 (n = 52) or inherited thrombocytopenia (IT; n = 20). Events requiring transfusions were 66% in IPFD, 5.7% in VWD-1, and 3% in IT. Baseline BS was significantly higher in IPFD patients with a bleeding event at follow-up than in those without (p < .01) and the percentage of subjects suffering a bleeding event increased proportionally to baseline BS quartile. A significant association between the BS and the chance of suffering severe bleeding was found in the overall, IPFD, and VWD-1 populations. Similar results were obtained for the pediatric population.Conclusions Inherited platelet function disorder patients with high BS at enrollment are more likely to suffer from bleeding events requiring treatment at follow-up. Moreover, the higher the baseline BS quartile the greater the incidence of subsequent events, suggesting that independently from diagnosis a high BS is associated with a greater risk of subsequent hemorrhage.
Показать больше [+] Меньше [-]Библиографическая информация
Эту запись предоставил Institut national de la recherche agronomique